HUE059557T2 - Prolyl hydroxylase inhibitors and methods of use - Google Patents

Prolyl hydroxylase inhibitors and methods of use

Info

Publication number
HUE059557T2
HUE059557T2 HUE18158907A HUE18158907A HUE059557T2 HU E059557 T2 HUE059557 T2 HU E059557T2 HU E18158907 A HUE18158907 A HU E18158907A HU E18158907 A HUE18158907 A HU E18158907A HU E059557 T2 HUE059557 T2 HU E059557T2
Authority
HU
Hungary
Prior art keywords
prolyl hydroxylase
hydroxylase inhibitors
methods
hif
anemia
Prior art date
Application number
HUE18158907A
Other languages
Hungarian (hu)
Inventor
Richard Masaru Kawamoto
Namal Warshakoon
Shengde Wu
Angelique Boyer
Kenneth Greis
Original Assignee
Akebia Therapeutics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38728868&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HUE059557(T2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Akebia Therapeutics Inc filed Critical Akebia Therapeutics Inc
Publication of HUE059557T2 publication Critical patent/HUE059557T2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4433Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/60Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/57Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and carboxyl groups, other than cyano groups, bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/65One oxygen atom attached in position 3 or 5
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/192Radicals derived from carboxylic acids from aromatic carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

The present disclosure relates to HIF-lα prolyl hydroxylase inhibitors, compositions which comprise the HIF-lα prolyl hydroxylase inhibitors described herein and to methods for controlling, inter alia, Peripheral Vascular Disease (PVD), Coronary Artery Disease (CAD), heart failure, ischemia, and anemia.
HUE18158907A 2006-06-26 2007-06-26 Prolyl hydroxylase inhibitors and methods of use HUE059557T2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US81652206P 2006-06-26 2006-06-26

Publications (1)

Publication Number Publication Date
HUE059557T2 true HUE059557T2 (en) 2022-11-28

Family

ID=38728868

Family Applications (2)

Application Number Title Priority Date Filing Date
HUE15191470A HUE041300T2 (en) 2006-06-26 2007-06-26 Prolyl hydroxylase inhibitors and methods of use
HUE18158907A HUE059557T2 (en) 2006-06-26 2007-06-26 Prolyl hydroxylase inhibitors and methods of use

Family Applications Before (1)

Application Number Title Priority Date Filing Date
HUE15191470A HUE041300T2 (en) 2006-06-26 2007-06-26 Prolyl hydroxylase inhibitors and methods of use

Country Status (26)

Country Link
US (14) US7811595B2 (en)
EP (6) EP3323807A1 (en)
JP (1) JP5113838B2 (en)
KR (1) KR101130592B1 (en)
CN (1) CN101506149B (en)
AT (1) ATE485264T1 (en)
AU (1) AU2007265460B2 (en)
BR (1) BRPI0713350B1 (en)
CA (1) CA2659682C (en)
CO (1) CO6170355A2 (en)
CY (1) CY1112021T1 (en)
DE (1) DE602007009992D1 (en)
DK (3) DK2044005T3 (en)
ES (3) ES2705587T3 (en)
HK (3) HK1129369A1 (en)
HU (2) HUE041300T2 (en)
IL (1) IL196127A (en)
LT (1) LT3357911T (en)
MX (1) MX2009000286A (en)
NZ (3) NZ601730A (en)
PL (3) PL3357911T3 (en)
PT (3) PT2044005E (en)
RU (1) RU2429226C9 (en)
SI (2) SI2044005T1 (en)
TR (1) TR201900548T4 (en)
WO (1) WO2008002576A2 (en)

Families Citing this family (84)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2468083C (en) 2001-12-06 2016-02-23 Fibrogen, Inc. Use of heterocyclic carboxamides to treat anemia
US7588924B2 (en) * 2006-03-07 2009-09-15 Procter & Gamble Company Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase
PT2044005E (en) 2006-06-26 2010-12-17 Warner Chilcott Co Llc Prolyl hydroxylase inhibitors and methods of use
JP5557832B2 (en) * 2008-03-18 2014-07-23 メルク・シャープ・アンド・ドーム・コーポレーション Substituted 4-hydroxypyridine-5-carboxamide
WO2009131129A1 (en) * 2008-04-22 2009-10-29 第一三共株式会社 5-hydroxypyrimidine-4-carboxamide compound
PT2294066E (en) * 2008-04-28 2014-11-21 Janssen Pharmaceutica Nv Benzoimidazoles as prolyl hydroxylase inhibitors
EP2273879A4 (en) * 2008-04-30 2012-03-21 Glaxosmithkline Llc Prolyl hydroxylase inhibitors
US8492398B2 (en) * 2008-05-08 2013-07-23 Merck Sharp & Dohme Corp. Spiroazaindoles
GB0809262D0 (en) 2008-05-21 2008-06-25 Isis Innovation Assay
JP5693452B2 (en) 2008-08-04 2015-04-01 シーエイチディーアイ ファウンデーション,インコーポレーテッド Specific kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions and methods of their use
WO2010085968A1 (en) * 2008-12-30 2010-08-05 European Molecular Biology Laboratory (Embl) Toluidine sulfonamides and their use as hif-inhibitors
ES2548250T3 (en) * 2009-02-10 2015-10-15 Janssen Pharmaceutica, N.V. Quinazolinones as prolylhydroxylase inhibitors
KR20180042443A (en) * 2009-07-17 2018-04-25 니뽄 다바코 산교 가부시키가이샤 Triazolopyridine compound, and action thereof as prolyl hydroxylase inhibitor and erythropoietin production inducer
JP5718236B2 (en) 2009-10-21 2015-05-13 第一三共株式会社 5-hydroxypyrimidine-4-carboxamide derivatives
RU2518071C2 (en) 2009-11-06 2014-06-10 Аэрпио Терапьютикс Инк. Prolyl hydroxylase inhibitors
CN102811620B (en) 2010-01-25 2015-03-25 Chdi基金会股份有限公司 Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
US10703722B2 (en) 2010-04-27 2020-07-07 Calcimedica, Inc. Compounds that modulate intracellular calcium
JP5755741B2 (en) * 2010-08-13 2015-07-29 ヤンセン ファーマシューティカ エヌ.ベー. 4-Aminoquinazolin-2-yl-1-pyrazole-4-carboxylic acid compounds as prolyl hydroxylase inhibitors
GB201102659D0 (en) 2011-02-15 2011-03-30 Isis Innovation Assay
NO2686520T3 (en) * 2011-06-06 2018-03-17
EP2717870B1 (en) * 2011-06-06 2017-09-27 Akebia Therapeutics Inc. Composition for stabilizing hypoxia inducible factor-2 alpha useful for treating cancer
GB201113101D0 (en) 2011-07-28 2011-09-14 Isis Innovation Assay
AU2012302144B2 (en) 2011-08-30 2017-06-15 Chdi Foundation, Inc. Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
MX2014002459A (en) 2011-08-30 2014-04-10 Chdi Foundation Inc Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof.
IN2014DN03155A (en) 2011-10-25 2015-05-22 Janssen Pharmaceutica Nv
CN104470899B (en) * 2012-03-09 2017-12-26 菲布罗根有限公司 The 4 isoquinolinol compounds as HIF hydroxylase inhibitors
TW201400458A (en) * 2012-03-30 2014-01-01 Daiichi Sankyo Co Ltd (2-heteroarylamino) succinic acid derivatives
NZ704147A (en) * 2012-07-30 2017-04-28 Taisho Pharmaceutical Co Ltd Partially saturated nitrogen-containing heterocyclic compound
US9040522B2 (en) * 2013-03-29 2015-05-26 Takeda Pharmaceutical Company Limited 6-(5-hydroxy-1H-pyrazol-1-yl)nicotinamide inhibitors of PHD
MX2020006963A (en) * 2013-06-13 2022-03-30 Akebia Therapeutics Inc Compositions and methods for treating anemia.
JP2016529257A (en) * 2013-08-16 2016-09-23 オハイオ ステート イノベーション ファウンデーション Compositions and methods for modulating DNA methylation
WO2015073779A1 (en) 2013-11-15 2015-05-21 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid, compositions, and uses thereof
CN106132201A (en) * 2014-01-23 2016-11-16 阿克比治疗有限公司 For treating compositions and the method for ocular disease
US9388135B2 (en) 2014-02-19 2016-07-12 Aerpio Therapeutics, Inc. Process for preparing N-benzyl-3-hydroxy-4-substituted-pyridin-2-(1H)-ones
JP2017114765A (en) * 2014-04-25 2017-06-29 大正製薬株式会社 Heteroaryl compound substituted with triazolyl
TR201815058T4 (en) 2014-07-11 2018-11-21 Grifols Worldwide Operations Ltd TRANSFERRIN FOR USE IN THE TREATMENT OF HYPOXY INDUCED FACTOR (HIF) RELATED NEURODEGENERATIVE DISORDERS.
PE20170770A1 (en) 2014-07-17 2017-07-04 Chdi Foundation Inc METHODS AND COMPOSITIONS FOR TREATING HIV-RELATED DISORDERS
WO2016029136A1 (en) * 2014-08-21 2016-02-25 Northwestern University 3-amidobenzamides and uses thereof for increasing cellular levels of a3g
US10065928B2 (en) 2014-09-02 2018-09-04 Sunshine Lake Pharma Co., Ltd. Quinolinone compound and use thereof
WO2016054806A1 (en) * 2014-10-10 2016-04-14 Merck Sharp & Dohme Corp. Substittued pyridine inhibitors of hif prolyl hydroxylase
CN104276999A (en) * 2014-10-10 2015-01-14 中国药科大学 Preparation method and intermediate of 3-hydroxyl-5-aryl pyridine-2-formamide derivative
JP2018039733A (en) * 2014-12-22 2018-03-15 株式会社富士薬品 Novel heterocyclic derivative
CN107427503A (en) * 2015-01-23 2017-12-01 阿克比治疗有限公司 The solid form, its composition and purposes of 2 (5 (3 fluorophenyl) 3 pyridone formamide) acetic acid
CN111773391A (en) 2015-02-27 2020-10-16 钙医学公司 Treatment of pancreatitis
EP3270922A4 (en) * 2015-03-20 2018-08-01 Akebia Therapeutics Inc. Deuterium-enriched hypoxia-inducible factor prolyl hydroxylase enzyme inhibitors
CN106146395B (en) * 2015-03-27 2019-01-01 沈阳三生制药有限责任公司 3- hydroxypyridine compound, preparation method and its pharmaceutical applications
CN107645953B (en) 2015-04-01 2022-11-01 阿克比治疗有限公司 Compositions and methods for treating anemia
AU2016306301B2 (en) 2015-08-07 2021-02-11 Calcimedica, Inc. Use of CRAC channel inhibitors for the treatment of stroke and traumatic brain injury
CN105039558B (en) * 2015-08-11 2018-06-15 中国农业科学院兰州畜牧与兽药研究所 Ox HIF-1A gene transcription level fluorescent quantificationally PCR detecting kits
CN105130888A (en) * 2015-10-09 2015-12-09 中国药科大学 Pyridylacetylene prolyl hydroxylase inhibitor and preparation method and medical application thereof
EP3400003B1 (en) * 2016-01-05 2023-05-03 The Trustees of Columbia University in the City of New York Compositions for regulating activity of inhibitor of dna binding-2 (id2) protein
CN105837502A (en) * 2016-04-05 2016-08-10 湖南欧亚生物有限公司 Synthesis method of Vadadustat
KR20190093651A (en) * 2016-12-13 2019-08-09 크리스탈 파마슈티컬 (쑤저우) 씨오., 엘티디. Novel crystalline forms of ((5- (3-chlorophenyl) -3-hydroxypyridine-2-carbonyl) amino) acetic acid and preparation methods thereof
WO2019028150A1 (en) 2017-08-01 2019-02-07 Akebia Therapeutics, Inc. Compositions for use in methods of treatment of hemoglobin disorders
CN107417605A (en) * 2017-08-02 2017-12-01 江苏艾立康药业股份有限公司 Act on the pyridine derivative compound of prolyl hydroxylase
WO2019036024A1 (en) 2017-08-17 2019-02-21 Bristol-Myers Squibb Company 2-(1,1 '-biphenyl)-1 h-benzo[d]imidazole derivatives and related compounds as apelin and apj agonists for treating cardiovascular diseases
MX2020011845A (en) 2018-05-09 2021-01-15 Akebia Therapeutics Inc Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2- carbonyl]amino]acetic acid.
CN110903238B (en) * 2018-09-14 2022-05-27 广东东阳光药业有限公司 Preparation method of kovar stat
WO2020075199A1 (en) 2018-10-12 2020-04-16 Mylan Laboratories Limited Polymorphic forms of vadadustat
CN111205222B (en) * 2018-11-21 2024-02-06 广东东阳光药业股份有限公司 Process for preparing pyridine ring compound
EP3887356B1 (en) 2018-11-28 2023-08-02 Sandoz AG Multi-component crystals of an orally available hif prolyl hydroxylase inhibitor
CN111320577B (en) * 2018-12-13 2023-06-23 广东东阳光药业有限公司 Preparation method and application of pyridine amide
CN109879804B (en) * 2019-01-30 2022-06-17 中国药科大学 5-heterocyclic substituted pyridine-2-formyl glycine compound, preparation method and medical application thereof
WO2020156571A1 (en) * 2019-02-02 2020-08-06 杭州华东医药集团新药研究院有限公司 Pyridazine derivative, and preparation method and medicinal use thereof
JP7470106B2 (en) 2019-04-26 2024-04-17 株式会社カネカ Method for preparing vadadustat intermediates
WO2020237374A1 (en) * 2019-05-28 2020-12-03 Montreal Heart Institute Picolinic acid derivatives and use thereof for treating diseases associated with elevated cholesterol
CN110305143B (en) * 2019-07-19 2021-03-09 济南新科医药科技有限公司 Furan [2,3-c ] pyridine derivative and preparation method and application thereof
US11524939B2 (en) 2019-11-13 2022-12-13 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid
IT201900021960A1 (en) * 2019-11-22 2021-05-22 Isagro Spa Compounds with fungicidal activity, their agronomic compositions and related preparation method
CN112979541B (en) * 2019-12-17 2022-11-11 浙江大学 N- (3-hydroxypyridine-2-carbonyl) glycine-based antitumor drug sensitizer and application thereof
CN113387882A (en) * 2020-03-11 2021-09-14 东莞市东阳光仿制药研发有限公司 Preparation method of vatacostat and intermediate thereof
US20230218592A1 (en) * 2020-04-20 2023-07-13 Akebia Therapeutics, Inc. Treatment of viral infections, of organ injury, and of related conditions using a hif prolyl hydroxylase inhibitor or a hif-alpha stabilizer
US20230241044A1 (en) * 2020-05-29 2023-08-03 Zydus Lifesciences Limited Treatment for psoriasis and skin inflammatory diseases
IT202000014116A1 (en) 2020-06-12 2021-12-12 Olon Spa NEW CRYSTALLINE VADADUSTAT COMPOUND
CN116670131A (en) * 2020-08-14 2023-08-29 阿克比治疗有限公司 PHD inhibitor compounds, compositions, and methods of use
CN116472266A (en) * 2020-10-16 2023-07-21 苏中药业集团股份有限公司 Compounds as prolyl hydroxylase inhibitors and methods of making the same
WO2022150623A1 (en) 2021-01-08 2022-07-14 Akebia Therapeutics, Inc. Compounds and composition for the treatment of anemia
KR20230130035A (en) 2021-01-08 2023-09-11 아케비아 테라퓨틱스 인코포레이티드 Treatment methods using vadadustat
IL305861A (en) * 2021-03-19 2023-11-01 Zydus Lifesciences Ltd Treatment for sickle cell anaemia
WO2022238745A1 (en) * 2021-05-14 2022-11-17 Zydus Lifesciences Limited Topical pharmaceutical composition of hif prolyl hydroxylase inhibitors
EP4347022A1 (en) 2021-05-27 2024-04-10 Keryx Biopharmaceuticals, Inc. Pediatric formulations of ferric citrate
DE102021131345A1 (en) 2021-11-30 2023-06-01 Catensys Germany Gmbh Chain drive and sprocket with inverted teeth and an accidentally or intentionally different arcuate tooth profile
WO2023111985A1 (en) * 2021-12-17 2023-06-22 Akebia Therapeutics, Inc. Picolinamide compounds as selective phd1 inhibitors, compositions, and methods of use
WO2023111990A1 (en) * 2021-12-17 2023-06-22 Akebia Therapeutics, Inc. Selective phd1 inhibitor compounds, compositions, and methods of use

Family Cites Families (103)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4044049A (en) * 1968-01-19 1977-08-23 Merck & Co., Inc. Phenyl benzoic acid compounds
US3894920A (en) * 1971-12-21 1975-07-15 Sagami Chem Res Process for preparing alkyl-substituted 3,6-dihydro-o-dioxin derivatives
US4016287A (en) * 1972-07-17 1977-04-05 Boehringer Ingelheim Gmbh Dermatological compositions containing an acylamino-carboxylic acid or an alkyl ester thereof
DE2234399A1 (en) * 1972-07-17 1974-01-31 Thomae Gmbh Dr K SKIN PROTECTION PRODUCTS
TW219933B (en) * 1990-02-26 1994-02-01 Lilly Co Eli
US5405613A (en) * 1991-12-11 1995-04-11 Creative Nutrition Canada Corp. Vitamin/mineral composition
TW352384B (en) 1992-03-24 1999-02-11 Hoechst Ag Sulfonamido- or sulfonamidocarbonylpyridine-2-carboxamides, process for their preparation and their use as pharmaceuticals
DE4219158A1 (en) 1992-06-11 1993-12-16 Thomae Gmbh Dr K Biphenyl derivatives, pharmaceutical compositions containing them and processes for their preparation
JP3341926B2 (en) 1993-04-17 2002-11-05 ソニー株式会社 Image conversion device
US5643957A (en) * 1993-04-22 1997-07-01 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
DE59401923D1 (en) 1993-11-02 1997-04-10 Hoechst Ag Substituted heterocyclic carboxylic acid amide esters, their preparation and their use as medicaments
EP0650961B1 (en) * 1993-11-02 1997-03-05 Hoechst Aktiengesellschaft Substituted heterocyclic carboxylic acid amides, their preparation, and their use as medicaments
CA2138929A1 (en) * 1993-12-30 1995-07-01 Klaus Weidmann Substituted heterocyclic carboxamides, their preparation and their use as pharmaceuticals
DE4410480A1 (en) 1994-03-25 1995-09-28 Hoechst Ag Sulfonamidocarbonylpyridine-2-carboxylic acid ester amides and their pyridine N-oxides, processes for their preparation and their use as medicaments
DE4410423A1 (en) 1994-03-25 1995-09-28 Hoechst Ag Sulfonamidocarbonylpyridin-2-carboxamides and their pyridine N-oxides, processes for their preparation and their use as medicaments
IL135495A (en) 1995-09-28 2002-12-01 Hoechst Ag Intermediate compounds for the preparation of substituted quinoline-2-carboxylic acid amides
JPH09221476A (en) * 1995-12-15 1997-08-26 Otsuka Pharmaceut Co Ltd Medicinal composition
US6080767A (en) 1996-01-02 2000-06-27 Aventis Pharmaceuticals Products Inc. Substituted n-[(aminoiminomethyl or aminomethyl)phenyl]propyl amides
US6323227B1 (en) * 1996-01-02 2001-11-27 Aventis Pharmaceuticals Products Inc. Substituted N-[(aminoiminomethyl or aminomethyl)phenyl]propyl amides
WO1997041103A1 (en) 1996-04-30 1997-11-06 Hoechst Aktiengesellschaft 3-alkoxypyridine-2-carboxylic acid amide esters, their preparation and their use as drugs
DE19620041A1 (en) * 1996-05-17 1998-01-29 Merck Patent Gmbh Adhesion receptor antagonists
DE19650215A1 (en) * 1996-12-04 1998-06-10 Hoechst Ag 3-hydroxypyridine-2-carboxylic acid amide esters, their preparation and their use as medicaments
US6420427B1 (en) * 1997-10-09 2002-07-16 Ono Pharmaceutical Co., Ltd. Aminobutyric acid derivatives
DE19746287A1 (en) 1997-10-20 1999-04-22 Hoechst Marion Roussel De Gmbh Substituted isoquinoline-2-carboxylic acid amides, their preparation and their use as medicaments
EP1080075B1 (en) 1998-03-23 2004-08-11 Aventis Pharmaceuticals Inc. Piperididinyl and n-amidinopiperidinyl derivatives
WO2000074725A1 (en) 1999-06-04 2000-12-14 Dana-Farber Cancer Institute, Inc. Identification of compounds that modify transcriptional responses to hypoxia
JP2001048786A (en) * 1999-08-05 2001-02-20 Yamanouchi Pharmaceut Co Ltd Tricyclic heteroaryl derivative
US6589758B1 (en) * 2000-05-19 2003-07-08 Amgen Inc. Crystal of a kinase-ligand complex and methods of use
US6609354B1 (en) 2000-09-22 2003-08-26 Grainpro, Inc. Method for long term storage of a bulk biologically active commodity
US6855510B2 (en) * 2001-03-20 2005-02-15 Dana Farber Cancer Institute, Inc. Pharmaceuticals and methods for treating hypoxia and screening methods therefor
US6849718B2 (en) 2001-03-20 2005-02-01 Dana Farber Cancer Institute, Inc. Muteins of hypoxia inducible factor alpha and methods of use thereof
AU2002241154A1 (en) * 2001-03-21 2002-10-03 Isis Innovation Ltd. Assays, methods and means relating to hypoxia inducible factor (hif) hydroxylase
SE0101327D0 (en) * 2001-04-12 2001-04-12 Astrazeneca Ab New crystalline forms
US6566088B1 (en) * 2001-10-04 2003-05-20 Board Of Regents, The University Of Texas System Prolyl-4-hydroxylases
GB0124941D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
CA2468083C (en) 2001-12-06 2016-02-23 Fibrogen, Inc. Use of heterocyclic carboxamides to treat anemia
US7053046B2 (en) 2001-12-21 2006-05-30 Mcgrath Kevin Peptide activators of VEGF
EP1554394B1 (en) 2002-10-16 2009-12-16 Isis Innovation Limited Screening methods using a structural model of FIH
WO2004048383A1 (en) * 2002-11-21 2004-06-10 Eli Lilly And Company Mixed lineage kinase modulators
US7618940B2 (en) * 2002-12-06 2009-11-17 Fibrogen, Inc. Fat regulation
US8124582B2 (en) 2002-12-06 2012-02-28 Fibrogen, Inc. Treatment of diabetes
US7183287B2 (en) * 2003-04-03 2007-02-27 Pharmacia Corporation Substituted pyrimidinones
US8614204B2 (en) 2003-06-06 2013-12-24 Fibrogen, Inc. Enhanced erythropoiesis and iron metabolism
WO2005007192A2 (en) * 2003-06-06 2005-01-27 Fibrogen, Inc. Cytoprotection through the use of hif hydroxylase inhibitors
CN102977016B (en) * 2003-06-06 2015-01-14 菲布罗根有限公司 Nitrogen-containing heteroaryl compounds and their use in increasing endogeneous erythropoietin
JPWO2005108370A1 (en) * 2004-04-16 2008-03-21 味の素株式会社 Benzene compounds
NZ551632A (en) 2004-05-28 2009-09-25 Fibrogen Inc HIF prolyl hydroxylase activity assay
WO2005115984A2 (en) * 2004-05-31 2005-12-08 Tanabe Seiyaku Co., Ltd. Large conductance calcium-activitated k channel opener
JP2006011127A (en) 2004-06-28 2006-01-12 Toppan Printing Co Ltd Lens cover
CA2573185A1 (en) * 2004-07-14 2006-02-23 Ptc Therapeutics, Inc. Methods for treating hepatitis c
TW200616969A (en) * 2004-09-17 2006-06-01 Tanabe Seiyaku Co Imidazole compound
WO2006084210A2 (en) * 2005-02-04 2006-08-10 Regents Of The University Of California, San Diego Hif modulating compounds and methods of use thereof
US7588824B2 (en) * 2005-02-25 2009-09-15 The Regents Of The University Of California Hydrogen cyano fullerene containing proton conducting membranes
JP2006316054A (en) * 2005-04-15 2006-11-24 Tanabe Seiyaku Co Ltd High-conductance type calcium-sensitive k channel opening agent
DE102005019712A1 (en) 2005-04-28 2006-11-09 Bayer Healthcare Ag Dipyridyl-dihydropyrazolone and its use
JP5390184B2 (en) * 2005-06-06 2014-01-15 ファイブローゲン、インコーポレーテッド Improved treatment of anemia
DE602006014843D1 (en) 2005-06-15 2010-07-22 Fibrogen Inc USE OF HIF 1ALFA MODULATORS FOR THE TREATMENT OF CANCER
US20070154482A1 (en) * 2005-09-12 2007-07-05 Beth Israel Deaconess Medical Center Methods and compositions for the treatment and diagnosis of diseases characterized by vascular leak, hypotension, or a procoagulant state
WO2007038571A2 (en) 2005-09-26 2007-04-05 Smithkline Beecham Corporation Prolyl hydroxylase antagonists
WO2007047194A2 (en) 2005-10-11 2007-04-26 Dana-Farber Cancer Institute, Inc. Methods for treating mitf-related disorders
US7728130B2 (en) 2005-12-09 2010-06-01 Amgen Inc. Quinolone based compounds exhibiting prolyl hydroxylase inhibitory activity
EP1983823A1 (en) 2006-01-17 2008-10-29 VIB vzw Inhibitors of prolyl-hydroxylase 1 for the treatment of skeletal muscle degeneration
CA2635899A1 (en) * 2006-01-19 2007-07-26 Osi Pharmaceuticals, Inc. Fused heterobicyclic kinase inhibitors
ITMI20060179A1 (en) 2006-02-02 2007-08-03 Abiogen Pharma Spa PROCEDURE FOR RESOLUTION OF RACEMIC MIXTURES AND DIASTEREOISOMERIC COMPLEX OF A SOLVING AGENT AND UNANTIOMER OF INTEREST
US7588924B2 (en) 2006-03-07 2009-09-15 Procter & Gamble Company Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase
PE20071020A1 (en) 2006-03-07 2007-12-11 Smithkline Beecham Corp N-SUBSTITUTED GLYCINE DERIVATIVE COMPOUNDS AS PROLYL HYDROXYLASE INHIBITORS
US20090176825A1 (en) 2006-05-16 2009-07-09 Fitch Duke M Prolyl hydroxylase inhibitors
JO2934B1 (en) 2006-06-23 2015-09-15 سميث كلاين بيتشام كوربوريشن Prolyl Hydroxylase Inhibitors
PT2044005E (en) 2006-06-26 2010-12-17 Warner Chilcott Co Llc Prolyl hydroxylase inhibitors and methods of use
TW200845991A (en) 2007-01-12 2008-12-01 Smithkline Beecham Corp N-substituted glycine derivatives: hydroxylase inhibitors
TW200845994A (en) 2007-01-12 2008-12-01 Smithkline Beecham Corp N-substituted glycine derivatives: prolyl hydroxylase inhibitors
WO2008130508A1 (en) 2007-04-18 2008-10-30 Amgen Inc. Indanone derivatives that inhibit prolyl hydroxylase
CA2683758A1 (en) 2007-04-18 2008-10-30 Merck & Co., Inc. Novel 1,8-naphthyridine compounds
EP2150251B9 (en) 2007-05-04 2013-02-27 Amgen, Inc Thienopyridine and thiazolopyridine derivatives that inhibit prolyl hydroxylase activity
CA2685942A1 (en) 2007-05-16 2008-11-27 Merck & Co., Inc. Spiroindalones
JP2009017975A (en) * 2007-07-10 2009-01-29 Aruze Corp Game machine
TW200908984A (en) 2007-08-07 2009-03-01 Piramal Life Sciences Ltd Pyridyl derivatives, their preparation and use
EP2188295A4 (en) 2007-08-10 2011-11-16 Crystalgenomics Inc Pyridine derivatives and methods of use thereof
DE602007004609D1 (en) 2007-09-03 2010-03-18 Electrolux Home Prod Corp Door with choke coil system for a microwave oven
WO2009039321A1 (en) 2007-09-19 2009-03-26 Smithkline Beecham Corporation Prolyl hydroxylase inhibitors
WO2009039323A1 (en) 2007-09-19 2009-03-26 Smithkline Beecham Corporation Prolyl hydroxylase inhibitors
WO2009043093A1 (en) 2007-10-04 2009-04-09 Newsouth Innovations Pty Limited Hif inhibition
WO2009049112A1 (en) 2007-10-10 2009-04-16 Smithkline Beecham Corporation Prolyl hydroxylase inhibitors
WO2009067790A1 (en) 2007-11-26 2009-06-04 Uti Limited Partnership STIMULATION OF HYPOXIA INDUCIBLE FACTOR -1 ALPHA (HIF-1α) FOR THE TREATMENT OF CLOSTRIDIUM DIFFICILE ASSOCIATED DISEASE (CDAD), FOR INTESTINAL MOTILITY AND FOR DETECTING INFECTION
JP2011505367A (en) 2007-11-30 2011-02-24 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー Prolyl hydroxylase inhibitor
WO2009073497A2 (en) 2007-11-30 2009-06-11 Smithkline Beecham Corporation Prolyl hydroxylase inhibitors
WO2009073669A1 (en) 2007-12-03 2009-06-11 Fibrogen, Inc. Isoxazolopyridine derivatives for use in the treatment of hif-mediated conditions
JP2011507894A (en) 2007-12-19 2011-03-10 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー Prolyl hydroxylase inhibitor
WO2009086592A1 (en) 2008-01-04 2009-07-16 Garvan Institute Of Medical Research Method of increasing metabolism
WO2009089547A1 (en) 2008-01-11 2009-07-16 Fibrogen, Inc. Isothiazole-pyridine derivatives as modulators of hif (hypoxia inducible factor) activity
NO2686520T3 (en) 2011-06-06 2018-03-17
EP2717870B1 (en) 2011-06-06 2017-09-27 Akebia Therapeutics Inc. Composition for stabilizing hypoxia inducible factor-2 alpha useful for treating cancer
MX2020006963A (en) 2013-06-13 2022-03-30 Akebia Therapeutics Inc Compositions and methods for treating anemia.
WO2015073779A1 (en) 2013-11-15 2015-05-21 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid, compositions, and uses thereof
CN106132201A (en) 2014-01-23 2016-11-16 阿克比治疗有限公司 For treating compositions and the method for ocular disease
CN107427503A (en) 2015-01-23 2017-12-01 阿克比治疗有限公司 The solid form, its composition and purposes of 2 (5 (3 fluorophenyl) 3 pyridone formamide) acetic acid
EP3270922A4 (en) 2015-03-20 2018-08-01 Akebia Therapeutics Inc. Deuterium-enriched hypoxia-inducible factor prolyl hydroxylase enzyme inhibitors
CN107645953B (en) 2015-04-01 2022-11-01 阿克比治疗有限公司 Compositions and methods for treating anemia
WO2019028150A1 (en) 2017-08-01 2019-02-07 Akebia Therapeutics, Inc. Compositions for use in methods of treatment of hemoglobin disorders
MX2020011845A (en) 2018-05-09 2021-01-15 Akebia Therapeutics Inc Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2- carbonyl]amino]acetic acid.
CN111320577B (en) * 2018-12-13 2023-06-23 广东东阳光药业有限公司 Preparation method and application of pyridine amide
US11524939B2 (en) * 2019-11-13 2022-12-13 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid
US20230286918A1 (en) * 2020-07-02 2023-09-14 Akebia Therapeutics, Inc. Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat

Also Published As

Publication number Publication date
US8323671B2 (en) 2012-12-04
BRPI0713350B1 (en) 2022-04-12
DK3026044T3 (en) 2019-02-18
US8940773B2 (en) 2015-01-27
NZ601731A (en) 2014-04-30
HK1218548A1 (en) 2017-02-24
US11426393B2 (en) 2022-08-30
RU2429226C9 (en) 2013-11-10
EP3026044B1 (en) 2018-11-07
US20130203816A1 (en) 2013-08-08
CN101506149A (en) 2009-08-12
EP2044005A2 (en) 2009-04-08
HK1258159A1 (en) 2019-11-08
LT3357911T (en) 2022-08-10
US20190192494A1 (en) 2019-06-27
EP2044005B1 (en) 2010-10-20
EP3323807A1 (en) 2018-05-23
EP2327696A1 (en) 2011-06-01
US9598370B2 (en) 2017-03-21
DK2044005T3 (en) 2011-01-24
DE602007009992D1 (en) 2010-12-02
PL3026044T3 (en) 2019-04-30
BRPI0713350A2 (en) 2012-03-13
US20210137901A1 (en) 2021-05-13
TR201900548T4 (en) 2019-02-21
WO2008002576A2 (en) 2008-01-03
ES2922078T3 (en) 2022-09-07
ES2705587T3 (en) 2019-03-26
US20150119425A1 (en) 2015-04-30
US20100331374A1 (en) 2010-12-30
KR20090060264A (en) 2009-06-11
US20130245076A1 (en) 2013-09-19
IL196127A (en) 2013-12-31
PT2044005E (en) 2010-12-17
ES2354584T3 (en) 2011-03-16
KR101130592B1 (en) 2012-04-02
PL2044005T3 (en) 2011-04-29
US20230201178A1 (en) 2023-06-29
US20070299086A1 (en) 2007-12-27
EP2044005B8 (en) 2012-12-05
AU2007265460A1 (en) 2008-01-03
ATE485264T1 (en) 2010-11-15
DK3357911T3 (en) 2022-07-04
EP3357911B1 (en) 2022-05-11
EP3357911A1 (en) 2018-08-08
JP2009541486A (en) 2009-11-26
SI3357911T1 (en) 2022-10-28
EP3026044A1 (en) 2016-06-01
RU2009102220A (en) 2010-08-10
US20160009648A1 (en) 2016-01-14
NZ601730A (en) 2014-04-30
RU2429226C2 (en) 2011-09-20
HUE041300T2 (en) 2019-05-28
AU2007265460B2 (en) 2011-03-03
US20140057892A1 (en) 2014-02-27
CA2659682A1 (en) 2008-01-03
US11883386B2 (en) 2024-01-30
USRE47437E1 (en) 2019-06-18
SI2044005T1 (en) 2011-01-31
PT3026044T (en) 2019-01-23
MX2009000286A (en) 2009-03-20
US8343952B2 (en) 2013-01-01
CA2659682C (en) 2010-12-21
US8598210B2 (en) 2013-12-03
US8722895B2 (en) 2014-05-13
NZ623002A (en) 2015-08-28
CN101506149B (en) 2012-11-14
US20140045899A1 (en) 2014-02-13
EP4095127A1 (en) 2022-11-30
HK1129369A1 (en) 2009-11-27
US7811595B2 (en) 2010-10-12
WO2008002576A3 (en) 2008-07-03
US20100331303A1 (en) 2010-12-30
IL196127A0 (en) 2009-09-22
CY1112021T1 (en) 2015-11-04
EP3026044B8 (en) 2018-12-19
CO6170355A2 (en) 2010-06-18
US10729681B2 (en) 2020-08-04
PL3357911T3 (en) 2022-09-05
JP5113838B2 (en) 2013-01-09
PT3357911T (en) 2022-07-11
US20170189387A1 (en) 2017-07-06

Similar Documents

Publication Publication Date Title
HK1258159A1 (en) Prolyl hydroxylase inhibitors and methods of use
IN2012DN04949A (en)
WO2007026251A8 (en) Use of dual c-kit/fgfr3 inhibitors for treating multiple myeloma
NZ596583A (en) Substituted dihydropyrazolones for treating cardiovascular and haematological diseases
SG160425A1 (en) Methods, compositions, and formulations for preventing or reducing adverse effects in a patient
WO2008033562A3 (en) Kinase inhibitor compounds
MA30725B1 (en) ADMINISTRATION OF DIPEPTIDYL PEPTIDASE INHIBITORS
WO2008076427A3 (en) Naphthalenone compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof
WO2009158031A3 (en) Methods and compositions for therapeutic treatment
NO20092569L (en) Inhibitors of Akt activity
ATE529531T1 (en) GM3 SYNTHASE AS A THERAPEUTIC TARGET IN MICROVASCULAR COMPLICATIONS OF DIABETES
EA200900091A1 (en) NEW INDICATIONS FOR THE USE OF DIRECT THROMBIN INHIBITORS IN THE TREATMENT OF CARDIOVASCULAR DISEASES
EA201270325A1 (en) METHODS OF SARCOMA TREATMENT USING EPIMETABOLIC SHIFTING ADDITIVE (STAFF Q10)
TW200801032A (en) Azaheterocyclyl derivatives of androstanes and androstenes as medicaments for cardiovascular disorders
MY150745A (en) Isoserine derivatives for use as coagulation factor ixa inhibitors
HK1121083A1 (en) Methods for reducing blood pressure
WO2008059041A3 (en) Complementation of factor xi deficiency by factor v mutants
MY148254A (en) Tartrate derivatives for use as coagulation factor ixa inhibitors
WO2005027887A3 (en) Methods and compositions for improving endothelial function
AU2015201137B2 (en) Compositions and method for tissue preservation
TN2018000344A1 (en) Pharmaceutical composition comprising a beta blocker, a converting enzyme inhibitor and an antihypertensive or an nsaid
EP1994029A4 (en) Potassium channel inhibitors